Canonical Allele Identifier: CA2395758334
Gene: SLC25A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.19176682T= , CM000684.2:g.19176682T= GRCh38
NC_000022.10:g.19164195T= , CM000684.1:g.19164195T= GRCh37
NC_000022.9:g.17544195T= NCBI36
NG_033863.1:g.7182A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000215882.10:c.643A= MANE Select ENSP00000215882.5:p.Asn215=
ENST00000215882.9:c.643A= ENSP00000215882.5:p.Asn215=
ENST00000451283.5:c.334A= ENSP00000401480.1:p.Asn112=
ENST00000461267.1:n.789A=
ENST00000470922.5:n.785A=
NM_001256534.1:c.664A= NP_001243463.1:p.Asn222=
NM_001287387.1:c.334A= NP_001274316.1:p.Asn112=
NM_005984.4:c.643A= NP_005975.1:p.Asn215=
NR_046298.2:n.694A=
NM_005984.5:c.643A= MANE Select NP_005975.1:p.Asn215=
NM_001256534.2:c.664A= NP_001243463.1:p.Asn222=
NM_001287387.2:c.334A= NP_001274316.1:p.Asn112=
NR_046298.3:n.567A=